par Theranexus (EPA:ALTHX)
Update on the Theranexus' Batten-1 project in CLN3 Batten's disease
- A communication by BBDF and Theranexus of the promising results of the Batten-1 Phase I/II trial at the Child Neurology Society Annual Meeting in San Diego (California)
- Additional expanded use of miglustat providing positive signals on visual acuity in younger CLN3 patients
Lyon, France – Austin, Texas, United States – November 19, 2024 – 6 PM CET – Theranexus, a biopharmaceutical company innovating in the treatment of rare neurological diseases, and the Beyond Batten Disease Foundation (BBDF) presented the final and positive results of the Phase I/II trial to evaluate Batten-1 in 6 young adult patients with CLN3 Batten's disease after 18 months of treatment, at the Child Neurology Society Annual Meeting in San Diego, 11 to 14th November.
This presentation highlights the strong safety profile of miglustat in CLN3 Batten disease patients and underscores the positive efficacy data gathered during this trial. The findings demonstrate clear target engagement, a biological effect, and are suggestive of a stabilization of disease progression over the treatment period. All trial participants chose to continue receiving miglustat through the BBDF's early access program, with no safety concerns reported after two years of ongoing treatment.
Additionally, case reports from expanded use of miglustat in CLN3 Batten disease further support its potential as a disease-modifying therapy. These reports suggest a possible stabilization of visual acuity—a function critically impacted in CLN3 Batten disease, often leading to legal blindness by age 12. This information is encouraging, especially in light of discussions between Theranexus, BBDF, the FDA, and EMA on using visual acuity as the primary endpoint for the upcoming Phase III trial, aimed at supporting the drug's registration in the U.S. and Europe.
The clinicians who treated these patients as well as other younger patients with miglustat, are enthusiastic about these promising data. For Professor Gary Clark, the trial's principal investigator and Chief of Child Neurology at Texas Children's Hospital in Houston “these case reports on visual acuity, in conjunction with other personal positive observations on visual experience in younger patients, complement our Phase I/II trial results that support the prospective benefit of Batten-1 in the treatment of CLN3 Batten's disease. Upon confirmation in a larger trial, these results with Batten-1 will be a breakthrough in the management of CLN3 Batten disease.”
Mathieu Charvériat, CEO and Chairman of Theranexus concludes: “Our positive Phase 1/2 study, as well as very promising additional case reports of expanded use of miglustat with positive outcome on vision, strongly support the launch of our phase 3, as well as the selection as visual acuity as primary endpoint. As indicated before, we explore options to have the necessary resources for our pivotal Phase III trial, and notably through the future commercialization of our liquid formulation in Niemann-Pick Type C as recently announced.”
About Beyond Batten Disease Foundation
Beyond Batten Disease Foundation (BBDF) is the world's largest nonprofit organization dedicated to funding research for a treatment and cure for juvenile (CLN3) Batten disease. Since its inception in 2008, over $35 million has been invested in research by leveraging donations, co-funding and strategic partnerships. BBDF is spearheading a unique, cohesive strategy, incorporating independent scientific resources and collaboration with related organizations to drive research in juvenile Batten Disease. Today there is a treatment in sight. BBDF funded research has discovered a drug – Batten-1 – that slows the progression of the disease in Batten models. More information can be found at www.beyondbatten.org.
About Theranexus
Theranexus is an innovative biopharmaceutical company that emerged from the French Alternative Energies and Atomic Energy Commission (CEA). The company has a unique platform for the identification and characterization of advanced therapy drug candidates targeting rare neurological disorders and an initial drug candidate in clinical development for Batten disease.
Theranexus is listed on the Euronext Growth market in Paris (FR0013286259- ALTHX).
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Disclaimer
This press release contains certain forward-looking statements concerning Theranexus and its business, including its prospects and product candidate development. Such forward-looking statements are based on assumptions that Theranexus considers to be reasonable. However, there can be no assurance that the estimates contained in such forward-looking statements will be verified, which estimates are subject to numerous risks including the risks set forth in the universal registration document of Theranexus filed with the AMF on 30 April 2024 under number D.24-0382 (a copy of which is available on www.theranexus.com) and to the development of economic conditions, financial markets and the markets in which Theranexus operates. The forward-looking statements contained in this press release are also subject to risks not yet known to Theranexus or not currently considered material by Theranexus. The occurrence of all or part of such risks could cause actual results, financial conditions, performance or achievements of Theranexus to be materially different from such forward-looking statements. Theranexus expressly declines any obligation to update such forward-looking statements.